Duns Number:317134468
Device Description: Manual and automated enzyme immunoassay for the in-vitro diagnostic quantitative determina Manual and automated enzyme immunoassay for the in-vitro diagnostic quantitative determination of dopamine in human plasma and urine.
Catalog Number
EIA-4615
Brand Name
Dopamine ELISA
Version/Model Number
EIA-4615
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)
-
Device labeled as "Not made with natural rubber latex"
-
For Single-Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
CHQ
Product Code Name
CHROMATOGRAPHIC/FLUOROMETRIC METHOD, CATECHOLAMINES
Public Device Record Key
572e0ed1-eba8-437a-9548-8df6dba83f06
Public Version Date
March 30, 2020
Public Version Number
2
DI Record Publish Date
June 06, 2019
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 84 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 27 |